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Interaction between dyslipidaemia, oxidative stress and inflammatory response in patients with angiographically proven coronary artery disease

机译:血管造影证实的冠心病患者的血脂异常,氧化应激和炎症反应之间的相互作用

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Introduction: Coronary artery disease (CAD) is emerging as the biggest killer of the 21st century. A number of theories have been postulated to explain the aetiology of atherosclerosis. The present study attempts to elucidate the interaction, if any, between inflammation, oxidative stress and dyslipidaemia in CAD. Methods: A total of 753 patients undergoing angiography were evaluated and 476 were included in the study. The parameters studied included complete lipid profile, and apolipoprotein B, ferritin and nitric oxide (NO) levels. Statistical analysis was carried out to determine the interrelationship between these parameters and the best predictor of CAD risk. Cut-off points were determined from the receiver operating characteristics curves, and the specificity, sensitivity, positive predictive value, negative predictive value, odds ratio and confidence intervals were calculated. Results: The levels of the parameters studied increased with the stenotic state and a positive correlation was observed between ferritin, NO and apolipoprotein B. NO emerged as the most reliable predictor of CAD, with an area under the curve of 0.992 and sensitivity and specificity of 97 and 98%, respectively. Conclusion: Environmental and genetic risk factors for CAD interact in a highly complex manner to initiate the atherosclerotic process. These risk factors should be considered mutually inclusive, not exclusive when devising pharmacological interventions, as multi-factorial risk management is the cornerstone of CAD management.
机译:简介:冠状动脉疾病(CAD)逐渐成为21世纪的最大杀手。已经提出了许多理论来解释动脉粥样硬化的病因。本研究试图阐明CAD中炎症,氧化应激和血脂异常之间的相互作用(如果有的话)。方法:总共评估了753例接受血管造影的患者,其中476例被纳入研究。研究的参数包括完整的脂质分布,载脂蛋白B,铁蛋白和一氧化氮(NO)水平。进行统计分析以确定这些参数与CAD风险的最佳预测指标之间的相互关系。从接收器的工作特性曲线确定截止点,并计算特异性,敏感性,阳性预测值,阴性预测值,比值比和置信区间。结果:所研究的参数水平随狭窄状态而增加,并且铁蛋白,NO和载脂蛋白B之间呈正相关。NO成为CAD的最可靠预测指标,其面积在0.992以下,灵敏度和特异性均在0.92以下。分别为97%和98%。结论:CAD的环境和遗传风险因素以高度复杂的方式相互作用,从而引发动脉粥样硬化过程。在设计药理干预措施时,应将这些风险因素考虑在内,而不是互斥,因为多因素风险管理是CAD管理的基石。

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